Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT04054843 |
Other study ID # |
Afamin in GDM |
Secondary ID |
|
Status |
Completed |
Phase |
|
First received |
|
Last updated |
|
Start date |
September 1, 2019 |
Est. completion date |
March 15, 2020 |
Study information
Verified date |
December 2020 |
Source |
Etlik Zubeyde Hanim Women's Health Care, Training and Research Hospital |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
This study includes pregnancies in 11 to 14 th gestational weeks. Investigators will sample
maternal plasma in the first trimester and analyze maternal plasma afamin values. All these
women will then be screened by two step OGTT. Investigators will compare afamin levels in GDM
and control groups.
Description:
Background Gestational diabetes mellitus (GDM) is an endocrinopathy that occurs during
pregnancy, and presents several clinical findings together with increased blood glucose
levels. The frequency of GDM differs, while the incidence of the disease in Turkey is
reported to be 7%. Most of the societies recommend screening all women with or without any
risk factors in terms of GDM. The definitive diagnosis is made via oral glucose challenge
test (OGTT). Early diagnosis and treatment are the key points to improve maternal and fetal
outcomes. Different biomarkers are studied regarding GDM diagnosis starting from first
trimester. However, there is not a worldwide accepted biomarker for defining the high risk
group to the date. Afamin is known as an important indicator of oxidative stress. Moreover,
oxidative stress itself is strongly associated with insulin resistance and obesity which are
responsible from GDM pathogenesis.
Objective To investigate the association between first trimester maternal plasma afamin
levels and GDM. Also, investigators aimed to understand the role of afamin for the prediction
of GDM in this study.
Methods This is an observational prospective cohort study conducted in Department of
Perinatology, Etlik Zubeyde Hanim Women's Health Care, Training and Research Hospital,
University of Health Sciences, Ankara, Turkey. During 11 and 14 weeks of gestational,
maternal blood will be obtained from eligible pregnant women, and samples will be stored at
-80 oC. Informed written consent will be obtained from participants. Between 24th and 28th
gestational weeks, all these women will be screened by two step OGTT. Then, afamin levels
will be compared in GDM and control groups. Exclusion criteria are; multiple pregnancy, fetal
anomalies, pregestational diabetes, underlying chronic diseases (hypertension, thyroid
dysfunction, other endocrinopathies, autoimmune disorders), age <18 or > 35 years, fasting
glucose level > 105 mg/dL or random glucose level > 200 mg/dL.